The U.S. Food and Drug Administration has finalized new warning labels for over-the-counter painkillers, warning consumers of the risks of stomach bleeds or liver damage related to the drugs. The new rules apply to acetaminophen (found in Tylenol) and non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen (Advil, Motrin), and naproxen (Aleve). The FDA said manufacturers must make sure that the active ingredients of these medications are prominently displayed on the drug labels on both...
Read moreWe frequently discuss that it's important for our doctors to know about any over-the-counter (OTC) medications we take for Migraines and... Read more »
Long term use of the painkiller ibuprofen when taken for more than five years has been found to decrease the risk of Alzheimer's disease by... Read more »
What exactly is a "black box" warning?Simply put, it's the strongest warning that the U.S. Food and Drug Administration (FDA) can require on a... Read more »
Officials with the U.S. Food and Drug Administration (FDA) have issued warnings to eight companies for illegally selling pain-relief gels that... Read more »
U.S. regulators want some over-the-counter (OTC) painkillers to have stronger warning labels. The new labels would warn consumers about the potential... Read more »
The U.S. Food and Drug Administration (FDA) has issued warnings to nine companies for selling 14 unapproved narcotic pain medicines as part of an... Read more »
The U.S. Food and Drug Administration (FDA) has ordered a new warning label for the cholesterol medication Zocor (simvastatin), saying that the drug... Read more »